In September 2021 the PHMPT sued the FDA for failure to respond to a FOIA request.  The FDA then asked the court to grant them permission to release only 500 pages per month.  On January 6, 2022, 18 months after the FOIA request, US District Judge Mark T. Pittman, Northern District of Texas, ordered the FDA to comply and “produce at least 55,000 pages per month” of the Pfizer documents they relied upon to license their COVID-19 vaccine in USA.

Since this time a huge “posse” of collaborating citizens, doctors and lawyers in a coordinated effort to review the Pfizer documents; which are revealing alarming insights into what was known before EUA was granted and shortly into the vaccine rollout!

Tracking the Pfizer FOIA documents – HERE